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Japanese multi institutional study of Primovist-enhanced MRI for non-invasive diagnosis of HCC (JAMP-HCC study)

Japanese multi institutional study of Primovist-enhanced MRI for non-invasive diagnosis of HCC (JAMP-HCC study) - Japanese multi institutional study of Primovist-enhanced MRI for non-invasive diagnosis of HCC (JAMP-HCC study)

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000011743
Enrollment
450
Registered
2013-09-14
Start date
2013-09-15
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

hepatic carcinoma

Interventions

Patients who suspected HCC are prospectively enrolled, and these patients will undergo contrast enhanced CT and EOB enhanced MRI (T1WI, T2WI, DWI, and enhanced T1WI).

Sponsors

Department of Radiology doctors' office, University of Yamanashi hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Step 1: Patients with final pathological diagnosis of liver tumors (including those other than HCC) for which EOB-enhanced MRI was performed before pathological diagnosis Inclusion criteria: Patients who meet all of the following criteria are included. 1.Patients who have chronic hepatic disease 2.Patients who underwent EOB-enhanced MRI 3. Patients with final pathological diagnosis of liver tumors (including those other than HCC) 4. Patients who are 20 years or older Step 2: Patients with suspected HCC who are expected to undergo EOB-enhanced MRI Inclusion criteria: Patients who meet all of the following criteria are included. 1. Patients who have chronic hepatic disease 2.Patients who are expected to undergo EOB-enhanced MRI and dynamic CT scan 3. Both inpatients and outpatients 4. Patients who are 20 years or older 5. Patients with clear consciousness

Exclusion criteria

Exclusion criteria: Step 1: Patients who meet any of the followingcriteria are not included in this study. 1. Patients who are judged to be inappropriate by the physician in charge Step 2: Patients who meet any of the following criteria are not included in this study. 1. Patients who are contraindicated or relatively contraindicated for iodine contrast agents and gadolinium contrast agents 2. Child-Pugh C 3. Patients with diffuse liver tumors 4. Patients who are judged to be inappropriate by the physician in charge (patients in terminal care, etc.)

Design outcomes

Primary

MeasureTime frame
Diagnosability (sensitivity, specificity, PPV, NPV, and positive/negative likelihood ratio) using typical findings of HCC by EOB-enhanced MRI (low signal intensity in the hepatocyte phase plus other findings) is compared to that of dynamic CT

Countries

Japan

Contacts

Public ContactTomoaki Ichikawa

University of Yamanashi hospital Department of Radiology

ichikawa@yamanashi.ac.jp055-273-1111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026